May 2, 2008
Pioneer® Surgical Technology Announces First Human Implants of its
NuNec™ Cervical Arthroplasty Device

March 25, 2008
Pioneer® Surgical Technology, Inc. Receives 510(k) Clearance to Market Next Generation Pedicle Screw System

February 29, 2008
Pioneer® Surgical Technology, Inc. Continues To Prove Science Behind Peek-On-Peek™ Technology for Motion Preservation Devices

October 24, 2007
Pioneer Surgical Technology Acquires Angstrom™ Medica, Inc.

October 19, 2007
Pioneer Surgical Technology Announces the Availability of its CLARITY™ Posterior Retractor System

July 2 , 2007
Pioneer Surgical Technology Enters License Agreement with AlpineSpine, LLC Pioneer Surgical to offer novel pedicle screw locking system

June 4, 2007
Pioneer Surgical Technology Acquires Encelle, Inc. Pioneer Surgical to Enter Orthobiologics Market

December 19, 2006
Pioneer Surgical Technology Closes $30.5 Million Preferred Equity Private Placement

October 5, 2006
Pioneer Surgical Technology Announces a New Agreement with Regeneration Technologies, Inc. to Distribute BioSet™ Demineralized Bone Matrix

August 31, 2006
Pioneer Surgical Technology Announces the Establishment of Its European Subsidiary in The Netherlands

August 31, 2006
Pioneer Victorious in Federal Appeals Court, Stryker Claim Dismissed

August 2, 2006
Pioneer Surgical Technology Begins NUBAC Intradiscal Arthroplasty™ System U.S. Clinical Trials for Patients With Degenerative Disc Disease

July 3, 2006
Pioneer Surgical Technology has received conditional approval from the FDA to proceed with clinical trials of its NUBAC ™ device. Pioneer plans to begin patient enrollment in the third quarter to assess the potential benefits of the NUBAC™ Disc Arthroplasty System.

March 31, 2006
Pioneer Surgical Technology and Encelle, Inc. have entered into an R&D collaboration for continuing the development of the E-MatrixTM product for use in spinal fusions.

December 21, 2005
Pioneer Surgical leads Michigan's new economy

August 8, 2005
Pioneer Surgical Technology announces its CE-mark approval for a unique motion preservation device indicated for degenerative disc disease.